US2024002593A1PendingUtilityA1
Production method for polyester copolymer comprising recycled monomers
Est. expiryOct 26, 2040(~14.2 yrs left)· nominal 20-yr term from priority
C08G 63/672C08G 63/199C08G 63/81C08G 63/183C08G 63/60Y02W30/62C08G 63/78
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Claims
Abstract
The present disclosure relates to a method for preparation of a polyester copolymer including recycled monomers, and to a method for preparation of a polyester copolymer having excellent quality while using recycled monomers.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method for preparation of a polyester copolymer comprising:
1) preparing a recycled bis-2-hydroxyethyl terephthalate solution by dissolving recycled bis-2-hydroxyethyl terephthalate in water or ethylene glycol (step 1); 2) preparing an oligomer by an esterification reaction of the recycled bis-2-hydroxyethyl terephthalate solution, a dicarboxylic acid or its derivative, and a diol containing ethylene glycol and a comonomer (step 2); and 3) preparing a polyester copolymer by a polycondensation reaction of the oligomer (step 3), wherein a molar ratio of the diol and the dicarboxylic acid or its derivative is 0.2:1 to 1.35:1.
2 . The method of claim 1 ,
wherein a concentration of the recycled bis-2-hydroxyethyl terephthalate solution is 25 to 99 wt %.
3 . The method of claim 1 ,
wherein the recycled bis-2-hydroxyethyl terephthalate is dissolved in water at 25 to 100° C. in step 1.
4 . The method of claim 1 ,
wherein the recycled bis-2-hydroxyethyl terephthalate is dissolved in ethylene glycol at 25 to 197° C. in step 1.
5 . The method of claim 1 ,
wherein the dicarboxylic acid or its derivative is terephthalic acid, dimethyl terephthalic acid, isophthalic acid, 2,6-naphthalenedicarboxylic acid, diphenyl dicarboxylic acid, 4,4′-stilbenedicarboxylic acid, 2,5-furandicarboxylic acid, or 2,5-thiophenedicarboxylic acid.
6 . The method of claim 1 ,
wherein the comonomer is cyclohexanedimethanol, or isosorbide.
7 . The method of claim 1 ,
wherein a molar ratio of the comonomer and ethylene glycol is 0.1:1 to 20:1 in step 2.
8 . The method of claim 1 ,
wherein the step 2 is performed at a pressure of 0.1 to 3.0 kg/cd and a temperature of 200 to 300° C.
9 . The method of claim 1 ,
wherein the step 2 is performed for 2 hours to 10 hours.
10 . The method of claim 1 ,
wherein the step 3 is performed at a temperature of 240 to 300° C. and a pressure of 400 to 0.01 mmHg.
11 . The method of claim 1 ,
wherein the step 3 is performed for 1 hour to 10 hours.
12 . The method of claim 1 ,
wherein the prepared polyester copolymer comprises 1 to 80 wt % of the residue of the recycled bis-2-hydroxyethyl terephthalate.
13 . The method of claim 1 ,
wherein the prepared polyester copolymer has an intrinsic viscosity of 0.50 to 1.0 dl/g.Join the waitlist — get patent alerts
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